{
"NDC": {
"NDCCode": "65219-510-20",
"PackageDescription": "25 VIAL, SINGLE-DOSE in 1 TRAY (65219-510-20) / 20 mL in 1 VIAL, SINGLE-DOSE (65219-510-02) ",
"NDC11Code": "65219-0510-20",
"ProductNDC": "65219-510",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Potassium Acetate",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Potassium Acetate",
"DosageFormName": "INJECTION, SOLUTION, CONCENTRATE",
"RouteName": "INTRAVENOUS",
"StartMarketingDate": "20241127",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA217515",
"LabelerName": "Fresenius Kabi USA, LLC",
"SubstanceName": "POTASSIUM ACETATE",
"StrengthNumber": "3.93",
"StrengthUnit": "g/20mL",
"Pharm_Classes": "Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2024-12-13",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20241127",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}